Structural brain correlates in major depression, anxiety disorders and post-traumatic stress disorder: A voxel-based morphometry meta-analysis
Creators
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Serra-Blasco, Maria1, 2, 3, 4
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Radua, Joaquim5, 6, 4
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Soriano-Mas, Carles7, 8, 4
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Gómez-Benlloch, Alba9
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Porta-Casteràs, Daniel1
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Carulla-Roig, Marta10
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Albajes-Eizagirre, Anton
- Arnone, Danilo11, 5
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Klauser, Paul12, 13
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Canales-Rodríguez, Eric J.14, 15, 4
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Hilbert, Kevin16
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Wise, Toby17
- Cheng, Yuqui18
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Kandilarova, Sevdalina19
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Mataix-Cols, David20, 21
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Vieta, Eduard6, 4
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Via, Esther10
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Cardoner, Narcís1, 8, 4
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1.
Institute of Research and Innovation Parc Tauli
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2.
Abat Oliba CEU University
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3.
Institut Català d'Oncologia
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4.
Instituto de Salud Carlos III
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5.
King's College London
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6.
Hospital Clínic de Barcelona
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7.
Institut d'Investigació Biomédica de Bellvitge
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8.
Autonomous University of Barcelona
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9.
Hospital General de Granollers
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10.
Hospital Sant Joan de Déu Barcelona
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11.
United Arab Emirates University
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12.
University Hospital of Lausanne
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13.
Monash University
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14.
Fidmag Sisters Hospitallers
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15.
École Polytechnique Fédérale de Lausanne
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16.
Humboldt-Universität zu Berlin
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17.
California Institute of Technology
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18.
First Affiliated Hospital of Kunming Medical University
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19.
Medical University Plovdiv
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20.
Karolinska Institute
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21.
Stockholm Health Care Services
Abstract
The high comorbidity of Major Depressive Disorder (MDD), Anxiety Disorders (ANX), and Posttraumatic Stress Disorder (PTSD) has hindered the study of their structural neural correlates. The authors analyzed specific and common grey matter volume (GMV) characteristics by comparing them with healthy controls (HC). The meta-analysis of voxel-based morphometry (VBM) studies showed unique GMV diminutions for each disorder (p < 0.05, corrected) and less robust smaller GMV across diagnostics (p < 0.01, uncorrected). Pairwise comparison between the disorders showed GMV differences in MDD versus ANX and in ANX versus PTSD. These results endorse the hypothesis that unique clinical features characterizing MDD, ANX, and PTSD are also reflected by disorder specific GMV correlates.
Additional Information
© 2021 Elsevier Ltd. Received 25 January 2021, Revised 6 June 2021, Accepted 5 July 2021, Available online 10 July 2021. PK was supported by a fellowship from the Adrian and Simone Frutiger Foundation. TW was supported by an NIHR PhD studentship and a Sir Henry Wellcome postdoctoral fellowship from the Wellcome Trust. EV was supported by a Río Hortega fellowship, provided by the Carlos III Health Institute (ISCIII), Spain (CM15/000839). NC has received research scholarships from Recercaixa, the Spanish Ministry of Health, the Ministry of Science and Innovation (CIBERSAM) and the Strategic Plan for Health Research and Innovation (PERIS)2016-2020.Attached Files
Supplemental Material - 1-s2.0-S0149763421003006-mmc1.docx
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Additional details
Identifiers
- Eprint ID
- 109963
- DOI
- 10.1016/j.neubiorev.2021.07.002
- Resolver ID
- CaltechAUTHORS:20210721-220520833
Related works
- Describes
- 10.1016/j.neubiorev.2021.07.002 (DOI)
Funding
- Adrian and Simone Frutiger Foundation
- National Institute for Health Research
- Wellcome Trust
- Carlos III Health Institute
- CM15/000839
- Recercaixa
- Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM)
- Strategic Plan for Health Research and Innovation (PERIS)
Dates
- Created
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2021-07-26Created from EPrint's datestamp field
- Updated
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2021-08-12Created from EPrint's last_modified field